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10.3892/ol.2015.3275 http://scihub22266oqcxt.onion/10.3892/ol.2015.3275 C4509032!4509032 !26622635     free     free     free Warning: file_get_contents(https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&id=26622635 &cmd=llinks): Failed to open stream: HTTP request failed! HTTP/1.1 429 Too Many Requests in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 215 Warning: imagejpeg(C:\Inetpub\vhosts\kidney.de\httpdocs\phplern\26622635 .jpg): Failed to open stream: No such file or directory in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 117       Oncol+Lett 2015 ; 10 (2 ): 1113-1116 Nephropedia Template TP {{tp|p=26622635 |t=2015. Glucagonoma syndrome: A case report |pdf=|usr=}}{{26622635 }} gab.com Text Glucagonoma syndrome: A case report JO: Oncol Lett http://www.kidney.de/pget.php?&tw=1&pmid=26622635 #FOAvip Necrolytic migratory erythema (NME), diabetes mellitus and glucagon-secreting tumors form the hallmarks of glucagonoma syndrome, and represent the major clinical manifestations of glucagonoma. NME is usually presented as the initial complaint of patients. Due to the rare incidence of glucagonoma, its diagnosis is often delayed, which leads to its progression. Here, we report a case of NME with a typical skin rash, which was misdiagnosed and treated with corticosteroids for two years. Removal of the tumor in the pancreatic body led to the rapid relief of the symptoms. The aim of the present study is to demonstrate the typical characteristics of glucagonoma syndrome to clinicians in order to improve its diagnosis and treatment. Twit Text FOAVip Glucagonoma syndrome: A case report ????Oncol Lett http://www.kidney.de/pget.php?&tw=1&pmid=26622635 #FOAvip Twit Text # Free Paper on # # # # # LINK http://www.kidney.de/pget.php?&tw=1&pmid=26622635 #FOAvip English Wikipedia <ref>{{Cite pmid|26622635 }}</ref> Glucagonoma syndrome: A case report #MMPMID26622635 Wei J ; Lin S ; Wang C ; Wu J ; Qian Z ; Dai C ; Jiang K ; Miao YI Oncol Lett 2015[Aug]; 10 (2 ): 1113-1116 PMID26622635 show ga Necrolytic migratory erythema (NME), diabetes mellitus and glucagon-secreting tumors form the hallmarks of glucagonoma syndrome, and represent the major clinical manifestations of glucagonoma. NME is usually presented as the initial complaint of patients. Due to the rare incidence of glucagonoma, its diagnosis is often delayed, which leads to its progression. Here, we report a case of NME with a typical skin rash, which was misdiagnosed and treated with corticosteroids for two years. Removal of the tumor in the pancreatic body led to the rapid relief of the symptoms. The aim of the present study is to demonstrate the typical characteristics of glucagonoma syndrome to clinicians in order to improve its diagnosis and treatment. äGlucagonoma syndrome: A case report (epmc).pdf DeepDyve Pubget Overpricing